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Interviewers

Interviewers are professionals who conduct interviews to gather information, assess skills, or evaluate candidates for various purposes such as employment, research, or data collection.
They use a range of techniques and strategies to effectively elicit responses, build rapport, and obtain accurate and relevant information from the interviewee.
Interviewers play a crucial role in streamlining the research process, enhancing reproducibility and accuracy of findings.
With the help of AI-powered platforms like PubCompare.ai, interviewers can easily locate protocols from literature, pre-prints, and patents, and leverage AI-driven comparisons to identify the best protocols and products, providing a seamiless research experince.

Most cited protocols related to «Interviewers»

Potential labels for the EQ-5D-5L were identified from a review of existing health-related quality-of-life instruments, a review of the literature on response scaling, hand searching of dictionaries and thesauruses, and informal interviews with native speakers of the target languages to establish how they described different severities of health problems. The same process was carried out in English and Spanish and, where possible, equivalent terms were sought in both languages. Labels included in the initial pool clearly had to fit with the lexical structure used in the EQ-5D-3L, such as ‘I have no problems doing my usual activities’ and ‘I have some problems doing my usual activities’.
In order to select labels from the pool for the new levels, an interviewer-administered response scaling exercise similar to those used in previous studies [14 (link), 19 , 20 (link)] was adopted to estimate the severity represented by each label. For this exercise, respondents were shown a rating scale in the form of a vertical, hash-marked, 40 cm visual analog scale (VAS) with end points of 0 and 100 to be used as a visual aid in grading label severity. For the Mobility, Self-Care and Usual Activities dimensions, the same set of labels was used. The interviewer placed a card labeled ‘No problems’, ‘No pain/discomfort’, or ‘No anxiety/depression’ as appropriate at the bottom of the scale (0) to act as the lower anchor and a card labeled ‘Unable to, ‘The worst pain or discomfort I can imagine’, ‘As anxious or depressed as I can imagine’ as the upper anchor (100). The respondent was then shown other labels from the pool singly in a quasi-random order and asked to assign a score between 0 and 100 to indicate label severity in relation to the lower and upper anchors.
The interviewer noted all scores, and when the respondent had rated all labels for a particular dimension, the interviewer laid them out in rank order alongside the VAS and asked the respondent to review the ranking and make any changes he or she thought necessary. If labels were reordered at this point, the respondent was asked to assign a new score to the relevant labels. Final scores assigned were recorded in an answer booklet. The scaling task was repeated for each dimension. Before finishing with the cards, the respondent was asked whether any of the labels sounded unusual, or should not be used in relation to a particular dimension.
Respondents rated labels for all five dimensions. The three functional dimensions (Mobility, Self-Care and Usual Activities) were always interspersed by the Pain/Discomfort and Anxiety/Depression dimensions, so that the respondent did not rate the same label types consecutively. Before rating the actual labels, respondents performed a practice task based on levels of overall health to get used to the study requirements. Data on age, level of education, main activity, and use of any current treatment for health problems, together with the existing EQ-5D-3L descriptive system and EQ-VAS, were collected after the response scaling task.
Before the main response scaling task, a pilot test was performed to test study procedures and materials. Based on the results of the pilot study, some labels were eliminated from the initial pool to achieve a more manageable number for the response scaling task. In particular, any labels using additional modifiers such as ‘very’ or ‘quite’ were eliminated as were any that were considered excessively colloquial or too high a level of language. After pilot testing, it was concluded that the feasible limit was about 10–12 labels per dimension for an individual respondent.
Responses to the scaling task were analyzed by calculating means and medians and the corresponding standard deviations and interquartile ranges (IQR). Labels to go forward for further testing were selected based on criteria that had been identified before data collection started. These included selecting labels close to or at the 25th, 50th, and 75th centiles on the VAS, ensuring consistency across dimensions and coherence with wording in the descriptive system. No quantitative comparison of label scores was carried out in deciding which labels to carry forward to the next stage; median scores were simply used as a guide to determine which labels fell closest to the 25th, 50th, and 75th centiles. Labels were also required to be in colloquial language. The choice of labels and their appropriateness was discussed by the task force at several meetings during the course of the study.
Publication 2011
Anxiety Hispanic or Latino Interviewers Marijuana Abuse Pain Range of Motion, Articular Visual Analog Pain Scale

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Publication 2010
Cardiovascular System Dental Health Services Diet Disabled Persons Family Structure Food Hearing Aids Hearing Impairment Hispanic or Latino Hispanics Interviewers Latinos Lung Diseases Malignant Neoplasms Mental Recall Tinnitus
The FFQ, originally developed for the TLGS, was a Willett-format questionnaire modified based on Iranian food items25 and contains questions about average consumption and frequency for 168 food items during the past year.7 The food items were chosen according to the most frequently consumed items in the national food consumption survey in Iran.25 Because different recipes are used for food preparation, the FFQ was based on food items rather than dishes, eg, beans, different meats and oils, and rice. Subjects indicated their food consumption frequencies on a daily basis (eg, for bread), weekly basis (eg, for rice and meat), monthly basis (eg, for fish), yearly basis (eg, for organ meats), or a never/seldom basis according to portion sizes that were provided in the FFQ. For each food item on the FFQ, a portion size was specified using USDA serving sizes (eg, bread, 1 slice; apple, 1 medium; dairy, 1 cup) whenever possible; if this was not possible, household measures (eg, beans, 1 tablespoon; chicken meat, 1 leg, breast, or wing; rice, 1 large, medium, or small plate) were chosen. Table 1shows food items and portion sizes used in the FFQ. Trained dietary interviewers with at least 3 of experience in the Nationwide Food Consumption Survey project25 or TLGS26 (link) administered the FFQs and 24-hour DRs during face-to-face interviews. The interviewer read out the food items on the FFQ, and recorded their serving size and frequency. The interview session took about 45 minutes. The interviewer for FFQ1 and FFQ2 was the same for each participant. Daily intakes of each food item were determined based on the consumption frequency multiplied by the portion size or household measure for each food item.27 The weight of seasonal foods, like some fruits, was estimated according to the number of seasons when each food was available.
Dietary data were also collected monthly by means of twelve 24-hour DRs that lasted for 20 minutes on average. For all subjects, 2 formal weekend day (Thursday and Friday in Iran) and 10 weekdays were recalled. All recall interviews were performed at subjects’ homes to better estimate the commonly used household measures and to limit the number of missing subjects. Detailed information about food preparation methods and recipe ingredients were considered by interviewers. To prevent subjects from intentionally altering their regular diets, participants were informed of the recall meetings with dietitians during the evening before the interview. All recalls were checked by investigators, and ambiguities were resolved with the subjects. Mixed dishes in 24-hour DRs were converted into their ingredients according to the subjects’ report on the amount of the food item consumed, thus taking into account variations in meal preparation recipes. For instance, broth or soup ingredients—usually vegetables (carrot or green beans), noodles, barley, etc.—differed according to subjects’ meal preparation. Because the only available Iranian food composition table (FCT)28 analyzes a very limited number of raw food items and nutrients, we used the USDA FCT29 as the main FCT; the Iranian FCT was used as an alternative for traditional Iranian food items, like kashk, which are not included in the USDA FCT.
The food items on the FFQ and DR were grouped according to their nutrient contents, based on other studies,30 (link) and modified according to our dietary patterns. Seventeen food groups were thus obtained, as follows: 1) whole grains, 2) refined grains, 3) potatoes, 4) dairy products, 5) vegetables, 6) fruits, 7) legumes, 8) meats, 9) nuts and seeds, 10) solid fat, 11) liquid oil, 12) tea and coffee, 13) salty snacks, 14) simple sugars, 15) honey and jams, 16) soft drinks, and 17) desserts and snacks (Table 1). The 168 food items on the FFQ were allocated to these 17 food groups, and the amounts in grams of each item were summed to obtain the daily intake of each food group.
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Publication 2010
Barley Bread Breast Carrots Cereals Chickens Coffee Dairy Products Diet Dietitian Eating Fabaceae Face Fishes Food Fruit Honey Households Hyperostosis, Diffuse Idiopathic Skeletal Interviewers Meat Mental Recall Monosaccharides Nutrients Nuts Oryza sativa Plant Embryos Potato Raw Foods Snacks Sodium Chloride, Dietary Soft Drinks Vegetables Whole Grains
Forty-eight out of 433 who participated in the first phase underwent IDIs from September 2017 to April 2018 at the National University of Singapore. Prior to the interviews, we asked for their willingness to participate in the IDIs in the survey questionnaire. We used the maximum variation sampling strategy to select a purposive sample from diverse backgrounds, based on sex and whether they reported meeting the recommendation. We created 4 matrices based on these criteria (i. female who reported meeting the recommendation, ii. female who reported not meeting the recommendation, iii. male who reported meeting the recommendation, and iv. male who reported not meeting the recommendation). We contacted participants who had indicated their interest earlier and also fulfilled the criteria for each of these matrices. Using the SEM as a framework, we conducted the interviews employing a topic guide based on whether they reported meeting the recommendation (Additional file 1). This was available in English, Malay and Mandarin. The guide was pilot tested before study commencement to allow smooth flow and coherence. The interviewers who were the first and seventh authors conducted the interviews according to the participant’s preferred language. This ranged from 30 min to an hour. The interviews were audio recorded with consent. We reached data saturation.
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Publication 2020
Interviewers Males Woman
We selected three existing qualitative datasets to which we applied the bootstrapping method. Although the datasets were all generated from individual interviews analyzed using an inductive thematic analysis approach, the studies from which they were drawn differed with respect to study population, topics of inquiry, sample heterogeneity, interviewer, and structure of data collection instrument, as described below.
Dataset 1. This study included 40 individual interviews with African American men in the Southeast US about their health seeking behaviors [29 (link)]. The interview guide contained 13 main questions, each with scripted sub-questions. Inductive probing was employed throughout all interviews. The inductive thematic analysis included 11 of the 13 questions and generated 93 unique codes. The study sample was highly homogenous.
Dataset 2. The second dataset consists of 48 individual interviews conducted with (mostly white) mothers in the Southeast US about medical risk and research during pregnancy [30 (link)]. The interview guide contained 13 main questions, each with scripted sub-questions. Inductive probing was employed throughout all interviews. Of note, the 48 interviews were conducted, 12 each, using different modes of data collection: in-person, by video (Skype-like platform), email (asynchronous), or text chat (synchronous). The qualitative thematic analysis included 10 of these questions and generated 85 unique codes.
Dataset 3. This study included 60 interviews with women at higher risk of HIV acquisition—30 participants in Kenya and 30 in South Africa [31 (link)]. The interview was a follow-up qualitative inquiry into women’s responses on a quantitative survey. Though there were 14 questions on the guide, only data from three questions were included in the thematic analysis referenced here. Those three questions generated 55 codes. Participants from the two sites were similar demographically with the exceptions of education and marital status. Substantially more women from the Kenya sample were married and living with their partners (63% versus 3%) and were less likely to have completed at least some secondary education. All interviews were conducted in a local language.
Data from all three studies were digitally recorded and transcribed using a transcription protocol [32 ]; transcripts were translated to English for Dataset 3. Transcripts were imported into NVivo [33 ] to facilitate coding and analysis. All three datasets were analyzed using a systematic inductive thematic approach [2 ], and all codes were explicitly defined in a codebook following a standard template [34 ]. For Datasets 1 & 2, two analysts coded each transcript independently and compared code application after each transcript. Discrepancies in code application were resolved through discussion, resulting in consensus-coded documents. For Dataset 3, two coders conducted this type of inter-coder reliability assessment on 20% of the interviews (a standard, more efficient approach than double-coding all interviews [2 ]). All three studies were reviewed and approved by the FHI 360 Protection of Human Subjects Committee; the study which produced Dataset 3 was also reviewed and approved by local IRBs in Kenya and South Africa.
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Publication 2020
African American Ethics Committees, Research Genetic Heterogeneity Homo sapiens Homozygote Interviewers Mothers Pregnancy Transcription, Genetic Woman

Most recents protocols related to «Interviewers»

We conducted key informant interviews with 28 respondents in the three refugee hosting districts. A semi-structured interview guide with open-ended questions and focused probes was used to guide the interviews. The guide consisted of several themes including: (a) elements of health services, (b) organisational factors on sustainability of health services (c) community and ecological factors and (d) funding. The questions emerged from literature review and the framework for sustainability of health services adopted to humanitarian health assistance. Interviews were conducted by trained research assistants. Interviews were conducted in English. Each interview lasted approximately between one to one and half hours. All interviews were audio-recorded with notes taken by interviewers.
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Publication 2023
Complement Factor B Interviewers Refugees
Firstly, before every interview, the respondents were made aware of the importance of their answers. The questionnaire was also designed to verify past responses with the following questions. In addition, interviewers were trained to detect incorrect answers by returning to some of the answers previously given by respondents and repeating some questions. This technique resulted in satisfactory responses from the mothers. However, after data collection, the forms were sorted to eliminate incorrect responses, poorly filled-out forms, and wrong answers.
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Publication 2023
Interviewers Mothers
This paper draws on interview-based research conducted from May to June 2022, as part of a broader project investigating how information about medicines moves between patients, pharmacists, and general practitioners. To explore how GP’s approached prescribing decisions and understood their relationships with patients and pharmacists around medicines, we elected to use an interview methodology. Interview methodologies are well-suited to research that investigates people’s thoughts and experiences, and the semi-structured format accommodates emergent findings that might not be anticipated in the original research design. The project received ethics approval from the Victoria University of Wellington Human Ethics Committee (#28324).
Given our aim to solicit general practitioners’ views specifically, we followed a purposive sampling strategy and recruited from a national pool, so as to gain cross-sectional insights from different geographic, socioeconomic, and institutional settings. Using the Medidata database of general practitioners, we issued an invitation for interview participants that reached 1,331 recipients. Of these, 25 people registered their interest via the supplied link, and 16 followed through to an interview. Our only selection criterion was that participants must be currently practicing general practitioners, as all 25 initial respondents were. Recruitment stopped when participants stopped opting in to the study.
While most of our resulting sample worked full-time in general practice, some of our interviewees worked part-time, as locums, or combined their general practice work with, e.g., working for hospice. Of our sixteen participants, 10 were female and six male. Eight were based in one of New Zealand’s three major cities, six in a smaller city or large town, and two rurally. Thus, while our sample is not representative, it does encompass a range of professional and regional experiences and clear themes were evident across the data set.
Interview guides were developed from the overall project’s aims, and included questions about participants’ professional backgrounds and contexts, prescribing practices and views on medicines, relationships to pharmacists, and perspectives on the New Zealand health system. In keeping with the semi-structured interview process, we allowed these guides to steer our conversations without dictating or unnecessarily limiting their course. The interview procedure was not adjusted in light of emergent findings, so as to ensure maximum comparability across the data set. However, the interview guide was adapted in some cases to suit individual participants’ time availability.
The authors conducted all interviews via Zoom, between May 1 and June 30 2022. Interviews lasted from 24 to 68 min, with a mean duration of 46 min 30 s. Typically, shorter interviews were those conducted during participants’ lunch breaks, and longer ones were conducted on participants’ days off or in the evenings. All interviews were audio recorded using the computer’s inbuilt recording software, then professionally transcribed verbatim. The original audio files and resulting transcripts were allocated pseudonymised alphanumeric file names (linked to identifying information in one securely stored spreadsheet) and stored in the University’s secure cloud storage system.
Although Denise Taylor training as a pharmacist could potentially be expected to influence how interviewees spoke about the pharmacists they interacted with, we did not note any discernible differences in the results collected by each interviewer, and neither had any existing relationship with any participants. It is possible that conducting interviews via Zoom also mitigated the extent to which the researchers’ positionality shaped interviews. We were known to participants’ primarily by our qualifications, professional roles, and association with a respected funder, with few cues as to our respective physical presentations beyond the shoulders-up Zoom window.
Our data analysis was conducted by (Courtney Addison) June through October 2023, and checked and discussed with Denise Taylor. Our analytic process was grounded in the constructivist tradition of Corbin and Strauss [34 ], which acknowledges the role of the analyst in meaning-making, and followed a Reflexive Thematic Analysis process [35 (link)]. This began with familiarisation with the data set (all interview transcripts), followed by iterative, open coding of the corpus. Codes were then reviewed and grouped into themes, which were themselves reviewed against the transcripts. The review process enabled refinements to the theme, so that, for example, the theme ‘Doctor/pharmacist interactions’ became ‘Sharing information about patients’, ‘Seeking medicines information’, ‘Correcting mistakes’. To check the validity of findings, the authors discussed transcripts and codes from their distinct disciplinary perspectives (Anthropology and Pharmacy, respectively) and also compared findings against the data set from the other arm of this project, which consists of interviews and observations from a community pharmacy. This confirmed, for example, that doctors were using pharmacists in the ways they described in the interviews reported on here, and that pharmacists were indeed picking up mistakes as interviewees report.
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Publication 2023
Ethics Committees General Practitioners Homo sapiens Hospice Care Interviewers Light Males Patients Pharmaceutical Preparations Physical Examination Physicians Shoulder Thinking Woman
Data for this study were drawn from two open prospective cohort studies of PWUD in Vancouver, Canada: the Vancouver Injection Drug Users Study (VIDUS) and the AIDS Care Cohort to evaluate Exposure to Survival Services (ACCESS). Both cohorts have been described in detail in previous literature [24 (link), 27 (link)]. However, to briefly summarize, these cohorts have been recruiting participants through community-based methods, including street outreach, self-referral, and word of mouth since May of 1996. VIDUS includes adults (18 years and older) who are HIV-negative and have injected unregulated drugs within the month prior to their enrolment. ACCESS participants are HIV-positive adults who used any unregulated substance (other than or in addition to cannabis) within the month prior to their enrolment. Participants in the VIDUS cohort who HIV seroconvert after their enrolment are transferred to the ACCESS cohort. All participants provided written informed consent at enrolment and ethics has been approved by Providence Health Care/University of British Columbia’s Research Ethics Board. Both cohorts use harmonized study protocols to facilitate pooled analyses.
At baseline and at 6-month intervals afterwards, participants complete interviewer- and nurse-led questionnaires and provide blood samples for serology, as well as urine for drug screening. The questionnaire covers a variety of topics including demographics, substance use, healthcare access, and socio-structural exposures. To compensate participants for their involvement, participants receive a $40 CAD stipend for every study visit.
Due to the COVID-19 pandemic, all in-person data collection was suspended between March 2020 and July 2020. After July 2020, infection control measures were put in place to resume data collection. Participant interviews were completed over telephone or videoconferencing. Study-owned cell phones and private spaces were loaned to those who required them. They were then able to pick up their cash honoraria in person or have it e-transferred if they had access to a bank account.
Between March and July of 2020, study questionnaires were modified to include questions regarding the COVID-19 pandemic. One of these questions was used to assess the primary outcome of this study, which read as follows: “Has the frequency of your use of these sites [i.e., SCS/OPS] changed since the beginning of the public health emergency?”. The outcome was dichotomized using the following responses: “I use them less” vs. “I use them more” or “My use stayed the same”. Potential correlates were identified based on past studies that assessed SCS access among PWUD [8 (link), 25 (link)], and included: age (per year older), self-identified gender (man vs. woman/other), ethnicity/ancestry (white vs. Black, Indigenous, and people of colour), education (high school or greater vs. other), employment (yes vs. no), residence in Downtown Eastside neighbourhood in Vancouver (yes vs. no), daily non-medical prescription opioid use (yes vs. no), daily cocaine use (yes vs. no), daily crystal methamphetamine use (yes vs. no), daily non-injection crack-cocaine use (yes vs. no), benzodiazepine use (yes vs. no), suspected that a drug used contained fentanyl (yes vs. no), used drugs alone (yes vs. no), engagement in opioid agonist therapy (yes vs. no), non-fatal overdose (yes vs. no), witnessed an overdose (yes vs. no), experience physical violence (yes vs. no), syringe/ drug use equipment sharing (yes vs. no), inability to access treatment (yes vs. no), unstable housing (yes vs. no), sex work (yes vs. no), incarceration (yes vs. no), jacked up (this refers to being stopped, searched, or detained) by the police (yes vs. no), cohort/ HIV status (ACCESS vs. VIDUS), ever tested positive for COVID-19 (yes vs. no), concern about COVID-19 on a scale from 1 to 10, with 10 indicating greatest concern (1–5 vs. 6–10), any chronic health conditions (yes vs. no), and ease of accessing SCS/OPS changed since COVID-19 (same vs. easier vs. harder). All drug use and behavioral variables refer to the 6 months prior to questionnaire date unless otherwise indicated.
Univariable and multivariable logistic regression analyses were used to assess the associations between the correlates of interest and reduced frequency of SCS/OPS use since COVID-19. Correlates of interest with a univariable p-value < 0.10 were included in a backward elimination procedure, with the least significant variable removed at each step until the lowest Akaike Information Criterion (AIC) was achieved. All p-values were two-sided and all statistical analyses were conducted using SAS version 9.4 (SAS Institute, Cary, North Carolina, United States).
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Publication 2023
Abuse, Physical Acquired Immunodeficiency Syndrome Adult Benzodiazepines BLOOD Cannabis Chronic Condition Cocaine COVID 19 Crack Cocaine Drug Abuser Drug Overdose Emergencies Ethnicity Fentanyl Gender Infection Control Interviewers Methamphetamine Nurses Opioids Oral Cavity Pharmaceutical Preparations Substance Use Urine Woman
Experienced research assistants from a survey firm recruited 215 heterosexual couples from Hungary. The eligibility criteria were that couples should: 1) have been cohabitating for at least one year, 2) be between 25 and 65 years old, 3) have no previous history of psychiatric disorders in the past five years, and that 4) at least one spouse has active working status. Two couples were excluded from the analysis for not meeting at least one of the criteria. For our final sample, 148 couples were available for the second wave of the study, while 65 couples refused or were unavailable.
The mean age was 39.72 years for men (SD = 10.40) and 38.57 years for women (SD = 10.00). The average relationship length was 17.10 years (SD = 9.99 years). Regarding relationship status, 64 couples (43.24%) were cohabiting without marriage, and 84 were married (56.75%). More than two-thirds (70.27%) of men and 68.92% of women reported to having at least one biological child (m = 1.41 for men and m = 1.42 for women, respectively). 18.07% of participants had earned college diplomas (16.89% of men and 19.26% of women), 63.85% had earned a high-school diploma (66.22% of men and 61.49% of women) and 16.89% had completed only primary education (20.95% of men and 12.84% of women).
Prior to the data assessment we acquired ethical approval from Semmelweis IRB (SE TUKEB). Potential participants were contacted at their homes. After both partners provided their informed consent, which included their inclusion in a one-year follow up, the interviewer administered the questionnaire pack and explicitly instructed the spouses to complete the assessment procedure separately. Then the interviewer left participants to fill out the survey by themselves, and recollected completed questionnaire pack at a later date agreed by phone. All data collected were handled confidentially. All partners that participated in the study voluntarily and received a book voucher for their contribution (6000 HUF, ~ US$20 per couple) in each wave of the study. Data sampling occurred from 2013 to 2014, which makes the sample unaffected by COVID-19 pandemic.
The same procedure was repeated one year later. To examine potential drop-out bias, we compared the sample of retained to lost couples. There were no differences in the goal-related or well-being variables under analysis at baseline. Regarding the demographic variables, we detected no difference in age, relationship status, numbers of children, or level of education, but couples who withdrew from the study had relationships shorter by three years on average (t(182) = -2.236, p = 0.027).
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Publication 2023
Biopharmaceuticals Child COVID 19 Eligibility Determination Heterosexuals Interviewers Mental Disorders Woman

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